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Institutional Review Board

The Institutional Review Board (IRB) at MidMichigan Health assures that all trials conducted at MidMichigan Health are in compliance with the standards of practice established by the Federal Food, Drug and Cosmetic Act and the U.S. Department of Health and Human Services for the protection of rights and welfare of human subjects.

How Do I Open a Study at MidMichigan?

Any provider or student currently working at MidMichigan Health may present a new study to the IRB for consideration by downloading and submitting the form entitled, Application for Initial Review of a Project Involving Human Subjects. Please contact the IRB coordinator with any questions.

Contact

Sandy Moore, R.N., IRB Coordinator
MidMichigan Medical Center - Midland
4000 Wellness Dr.
Midland, MI 48670
Phone (989) 488-5945
Email sandra.moore@midmichigan.org